- Edwards Lifesciences (Trenton, NJ)
- …subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good ... skills. + Providing input on strategic direction on field monitoring of studies and data collection for clinical...cardiology trials + Master's Degree in related field + Clinical research certification (ACRP or SoCRA … more
- Parexel (Trenton, NJ)
- …Specialist, Clinical Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience: Minimum 3 years ... (DSMM) + Partners with SCP and Country Study Operations Manager (SOM) + When required Partners with other Study...relevant experience in clinical research site monitoring (preferably 2 years in… more
- Parexel (Trenton, NJ)
- …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the ... delivery of the study. The CRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the ... delivery of the study. The SrCRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Senior Clinical Research Director **Location:** Cambridge, MA or Morristown, NJ **About the Job** Join the engine of Sanofi's mission - where deep ... the impossible into possible for millions. As the **Senior Clinical Research Director** (Senior CRD) within the...review of data within the scope of the Centralized monitoring , clinical and medical information for the… more
- Vitalief (New Brunswick, NJ)
- …in New Brunswick, NJ. Job Responsibilities: + Under the direct supervision of the Nurse Manager of Clinical Research Center (CRC), you will be responsible ... and managing patient care (patient retention). + Assist with monitoring patient visits. + Track deviations and documenting SAEs...Minimum of 1 to 2 years of experience in Clinical Research as a Clinical … more
- Regeneron Pharmaceuticals (Warren, NJ)
- …landscape + Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage ... The Senior Manager , Hematology, Clinical Scientist leads in...seeking proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research… more
- Merck (Trenton, NJ)
- …or business management is preferred. **Prerequisites:** + Minimum of 6 years in clinical research including at least 2 years with developing and managing ... up of regulatory inspections. **Operational Quality Management:** + The Clinical Quality Operations Manager is accountable for... Clinical Data Management, Clinical Development, Clinical Quality Management, Clinical Research ,… more
- Taiho Oncology (Princeton, NJ)
- …Under minimal supervision, leads and manages complex global studies to support the Clinical Development Plan. The Senior Study Manager (SSM) is responsible for ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
- Vitalief (New Brunswick, NJ)
- …partner working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise ... that ultimately benefit patients. We are seeking a problem-solving, "hands-on" Grants Manager to join our exceptional client team. WHY VITALIEF? + You can… more